Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:01 AM
Ignite Modification Date:
2025-12-25 @ 4:01 AM
NCT ID:
NCT00809302
Eligibility Criteria:
Inclusion Criteria:
* Male or female at least 30 years old;
* Initial diagnosis of idiopathic PD must be within 5 years;
* At least two of the following cardinal signs must be present: bradykinesia, resting tremor, and rigidity;
* PD progression must be Stage 1 to 2.5 (inclusive) according to the modified Hoehn and Yahr classification system;
* Have a score on the MoCA of at least 26;
* Have a score on the Beck Depression Inventory II (BDI II) of less than 15;
* Have a screening UPDRS (Part III) motor score of at least 10;
* In good general health as determined by a thorough medical history and physical examination (including vital signs), neurological examination, 12-lead ECG, and clinical chemistry laboratory tests;
* Females of childbearing potential must be using an acceptable method of contraception and have a negative serum pregnancy test at the screening and baseline visits. Acceptable methods of contraception are oral, intrauterine, implantable, injectable contraceptives, double barrier methods or condoms impregnated with spermicide. After screening, subjects using oral contraceptive methods of contraception must agree to add an additional method until 30 days after the last dose of study medication. Women on oral contraceptives or using cervical rings must have been using them for at least 1 month before the screening visit;
* Male subjects with partners of childbearing potential must use adequate contraception during the study and for 3 months after the study;
* Females receiving hormone replacement therapy must be on a stable regimen for at least 3 months;
* Able to read, understand, and provide written/dated informed consent before enrolling in the study, and must be willing to comply with all study procedures.
Exclusion Criteria:
* History or clinical features consistent with an atypical parkinsonian syndrome;
* History of surgical intervention for PD;
* History of severe allergic or anaphylactic reaction to any drug;
* History of allergies or known sensitivity, hypersensitivity, or severe adverse reaction (e.g., requiring abrupt discontinuation) to any drug similar to aplindore;
* Taking prescription drug therapy or over the counter medication for chronic medical conditions who have not been on stable doses for at least 1 month before the screening visit;
* Treated with L-dopa within 2 months before the baseline visit or who have had cumulative treatment exceeding 2 months;
* Have taken dopamine agonist therapy within 1 month before the baseline visit or who have taken dopamine agonist therapy for a cumulative period exceeding 2 months;
* Are receiving amantadine, anticholinergics, or monoamine oxidase B inhibitors who have not been taking stable doses for at least 2 months before the baseline visit;
* A clinically significantly abnormal clinical laboratory value as judged by the investigator or a value that is disapproved by the study Clinical Monitor;
* A decrease in either systolic blood pressure of at least 40 mmHg or a decrease in diastolic blood pressure of at least 20 mmHg following 5 minutes supine and 2 minutes standing, at or within 6 months before the baseline visit;
* Clinically significant ECG findings, including prolonged QTcF intervals (\>450 msec for men, \>470 msec for women);
* Evidence of clinically significant unstable allergic (except for untreated, asymptomatic, seasonal allergies at time of dosing), hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurological disease;
* History of basal or squamous cell skin cancers or carcinoma in situ of the cervix within 2 years before the screening visit are excluded; for all other cancer diagnoses, subjects with a history within 5 years before the screening visit are excluded;
* Any condition that may significantly affect drug absorption;
* Pregnant or lactating females;
* History or evidence of drug abuse or alcoholism as defined by DSM-IV TR within 12 months before the baseline visit or evidence of current withdrawal from drugs or alcohol before the baseline visit;
* Prior exposure to aplindore;
* Received any investigational drug within 60 days before the baseline visit.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
30 Years
Study:
NCT00809302
Study Brief:
Protocol Section:
NCT00809302